We are currently looking to recruit programmers for our client within their
Data Management Technology group. This is an excellent contract opportunity
for those with strong SAS Programming experience in a Clinical Trials
Environment. Roles can be based either in the North of England or in the
Midlands.
Description:
The post-holder will be responsible for the delivery of Data Management (DM)
technical activities in support of clinical studies, working closely with
study teams to:
Develop in-house database specifications
Develop edit check programming including ad hoc listings
Produce specifications, transfer file formats and processes for
transmission and loading of data files from external/third-party vendors
Assist with database technical verification
Co-ordinate deliverables from out-sourcing parties and external vendors
Minimum Requirements Education and Experience
Computing/life science degree or equivalent experience
Substantial experience in SAS programming in a clinical environment
Experience of computer systems validation methodology
Experience of working with clinical information and clinical development
processes
Knowledge of clinical and pharmaceutical drug development process and
associated GCP
Skills and Capabilities
Excellent analytical and problem solving skills
Good written and verbal communication skills, interpersonal skills
Excellent customer focus and good client relationship skills
Good presentation skills
Flexibility
Concern for standards
Delivery focused
Excellent team working skills
Ability to work as a member of a cross-functional team, with a large
degree of independence
Initiative
If interested in these or other opportunities please email your CV to
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